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Integration of molecular and enzymatic catalysts on graphene for biomimetic generation of antithrombotic species

Teng Xue, Bo Peng, Min Xue, Xing Zhong, Chin-Yi Chiu, Si Yang, Yongquan Qu, Lingyan Ruan, Shan Jiang, Sergey Dubin, Richard B. Kaner, Jeffrey I. Zink, Mark E. Meyerhoff (), Xiangfeng Duan () and Yu Huang ()
Additional contact information
Teng Xue: University of California
Bo Peng: The University of Michigan, 930 N. University
Min Xue: University of California
Xing Zhong: University of California
Chin-Yi Chiu: University of California
Si Yang: The University of Michigan, 930 N. University
Yongquan Qu: University of California
Lingyan Ruan: University of California
Shan Jiang: University of California
Sergey Dubin: University of California
Richard B. Kaner: University of California
Jeffrey I. Zink: University of California
Mark E. Meyerhoff: The University of Michigan, 930 N. University
Xiangfeng Duan: University of California
Yu Huang: University of California

Nature Communications, 2014, vol. 5, issue 1, 1-6

Abstract: Abstract The integration of multiple synergistic catalytic systems can enable the creation of biocompatible enzymatic mimics for cascading reactions under physiologically relevant conditions. Here we report the design of a graphene–haemin–glucose oxidase conjugate as a tandem catalyst, in which graphene functions as a unique support to integrate molecular catalyst haemin and enzymatic catalyst glucose oxidase for biomimetic generation of antithrombotic species. Monomeric haemin can be conjugated with graphene through π–π interactions to function as an effective catalyst for the oxidation of endogenous L-arginine by hydrogen peroxide. Furthermore, glucose oxidase can be covalently linked onto graphene for local generation of hydrogen peroxide through the oxidation of blood glucose. Thus, the integrated graphene–haemin–glucose oxidase catalysts can readily enable the continuous generation of nitroxyl, an antithrombotic species, from physiologically abundant glucose and L-arginine. Finally, we demonstrate that the conjugates can be embedded within polyurethane to create a long-lasting antithrombotic coating for blood-contacting biomedical devices.

Date: 2014
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Persistent link: https://EconPapers.repec.org/RePEc:nat:natcom:v:5:y:2014:i:1:d:10.1038_ncomms4200

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DOI: 10.1038/ncomms4200

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